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通过柱上 Suzuki 交叉偶联反应修饰寡脱氧核苷酸。

Modification of oligodeoxynucleotides by on-column Suzuki cross-coupling reactions.

机构信息

Biomolecular Nanoscale Engineering Center, Department of Physics, Chemistry and Pharmacy, University of Southern Denmark, DK-5230 Odense M, Denmark.

出版信息

Chem Commun (Camb). 2018 Jul 12;54(57):8003-8006. doi: 10.1039/c8cc01360h.

Abstract

The on-column functionalization of oligodeoxynucleotides via base-free Suzuki cross-coupling reactions is reported herein. These cross-coupling reactions were carried out with various boronic acids and either full-length modified oligonucleotides containing one or more 2'-deoxy-5-iodouridine (5IdU) monomer(s) or on oligonucleotide fragments immediately after incorporation of 5IdU. Five different functionalities were coupled to oligonucleotides containing one or three attachment points.

摘要

本文报道了通过无碱基 Suzuki 交叉偶联反应在寡脱氧核苷酸柱上进行的功能化。这些交叉偶联反应是用各种硼酸与全长修饰的寡核苷酸(含有一个或多个 2'-脱氧-5-碘尿苷(5IdU)单体)或在掺入 5IdU 后立即在寡核苷酸片段上进行的。将五种不同的功能基团偶联到含有一个或三个附着点的寡核苷酸上。

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